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EU Commission’s proposal amending the transition period of the MRD regulation

Manuele Cantù -
0

Unified Patent Court, the roadmap towards activation

Manuele Cantù -
1

Structured dialogue with the EU Commission to prevent shortages

Giuliana Miglierini -
0

ICH’s reflection paper and consultation on patient focused drug development

Giuliana Miglierini -
0

EMA and HMA’s new joint regulatory strategy

Giuliana Miglierini -
0

Regulatory sandboxes to experiment real-world innovation

Giuliana Miglierini -
0

Updates on the activities of the EU’s Pharmaceutical Committee

Giuliana Miglierini -
0

The EU Parliament approved the report on shortages of medicines

Giuliana Miglierini -
0

Europe goes for real-world studies and GMO vaccines

Giuliana Miglierini -
0

The industry asks for a mutual recognition agreement between the EU...

Giuliana Miglierini -
0
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